Job Description for Senior Quality Manager Key Responsibilities: Quality Control Management: Lead and oversee all quality control activities in the manufacturing process for hearables and wearables, ensuring product conformity with customer specifications and regulatory standards. Develop and implement inspection and testing protocols to monitor product quality at various stages of production. Manage the identification, investigation, and resolution of non-conformities, including root cause analysis and corrective/preventive actions (CAPA). Monitor and analyze quality metrics, identifying trends, and implementing corrective actions to ensure quality standards are consistently met. Quality Process Improvement: Drive continuous improvement initiatives using methodologies like Lean, Six Sigma, and other process optimization techniques. Identify and implement strategies to streamline manufacturing processes and improve product quality, efficiency, and cost-effectiveness. Foster a culture of continuous improvement across the quality team and production floor. Lead Kaizen events, root cause analysis, and other improvement programs. Team Leadership & Development: Lead, mentor, and manage a team of quality control inspectors, quality engineers, and other quality professionals. Conduct training and development programs to ensure the team is up to date with industry best practices, quality standards, and internal procedures. Encourage a team-oriented and proactive approach to problem-solving and quality assurance. Quality Management System (QMS) Implementation & Compliance: Ensure compliance with relevant international quality standards (ISO 9001, ISO 13485, IATF 16949, etc.) and industry-specific regulations. Oversee the implementation and maintenance of QMS, ensuring all procedures are followed and documented appropriately. Lead internal audits and support external audits as needed. Supplier & Customer Quality Management: Manage supplier quality relationships, conducting supplier audits, performance evaluations, and ensuring that suppliers meet company quality standards. Communicate directly with customers regarding quality concerns, non-conformance issues, and ensure timely resolution of quality-related complaints. Data Analysis & Reporting: Collect, analyze, and report on key quality performance indicators (KPIs) to senior management. Develop and implement data-driven strategies to track quality metrics, identify potential risks, and make informed decisions for process improvements.

Role & responsibilities Oversee the quality assurance team and processes for sheet metal production. Develop and implement quality control protocols and procedures. Conduct regular audits and inspections to ensure compliance with quality standards. Collaborate with production and engineering teams to identify and resolve quality issues. Drive continuous improvement initiatives to enhance product quality and operational efficiency. Perform root cause analysis and develop corrective action plans. Ensure compliance with industry regulations and standards. Train and mentor quality assurance staff. Continuously carry out Pre dispatch inspection Continuously carry out pre production inspection Maintaining Quality documentation Requirements Bachelor's degree in Mechanical Engineering, Industrial Engineering, or a related field. 2+ years of experience in quality assurance, with at least 3 years in a leadership role within the sheet metal industry. Strong knowledge of quality control methodologies, tools, and standards. Proven track record of successfully implementing quality improvement initiatives. Excellent problem-solving skills and attention to detail. Strong leadership and team management abilities. Effective communication and interpersonal skills. Skills Quality Management Systems (QMS) Root Cause Analysis Lean Manufacturing Auditing Corrective and Preventive Actions (CAPA)

Role & responsibilities To review and maintain production schedule as per the project/priority and as per the availability of the required material & all other related resources. Responsible for production related activities of Block and timey execution of production planning batches/activities Optimum utilization of man, material and machinery oi pharmaceutical products To deal with outside parties for changes, improvements in equipment, process which direct impact on product quality. To review and approve documents through QMS software if applicable, but not to, SOP, Change Centre, Planned Modification, Event and investigate reverts. Monthly/Quarterly/Half yearly/yearly report Study protocol and report, Qualification report and protocol.Other relevant documents as applicable. To review the document like MF, BMR (Batch Manufacturing Record), BOM (Bill of Material). Preferred candidate profile : Should be from Injectables background with USFDA experience

Roles and Responsibilities Quality assurance and ensure 100% system documentation and its compliance. Conduct internal audits, support MR, and work with process owners to track and close all non-conformances . Desired Candidate Profile Perks and Benefits Best as per the industry

Job Description To ensure all the products manufactured and distributed by the bottling operation conform to the specifications through assurance of processes from supply to consumer. The QAE supports the identification, planning, documentation, and management of the practices, activities and resources needed to meet quality goals and objectives in a manner that enables management to assess quality performance. Job Responsibilities Responsibility for all quality management, and quality assurance activities in the bottling operation. Responsibility for adherence to Company guidelines and requirements in the supply, manufacturing and distribution processes. Responsibility for the conformance to specifications of the finished goods leaving the plant. Responsibility to monitor, assess and improve process capabilities in the plant Responsibility for conducting the required tests on raw materials, packaging materials, WIP and finished product at the specified frequencies. Responsibility for availability and calibration of inspection and testing equipment and chemical reagents. Responsibility for process control of the final syrup, water treatment Responsibility for raw material, ingredient and product identification and traceability. Responsibility for the implementation of GMP in the plant. Responsibility to document, implement and monitor a quality assurance system in accordance with the KORE Requirements. - Commitment to Development Commitment to Excellence Teamwork Planning and Execution Influencing Knowledge of the Business Job Requirement Minimum Education: Post Graduate in Microbiology. Minimum Experience: 2 - 3 years in a Microbiology in beverage industry.

Skill required: Talent & HR - Talent Management Designation: Quality Auditing Specialist Qualifications: Any Graduation Years of Experience: 7 to 11 years What would you do? Improve workforce performance and productivity, boosts business agility, increases revenue and reduces costsTalent & HR processSupport workforce behavior in alignment with the organization`s business strategy by designing, developing, implementing, and executing key HR processes:strategic planning; supply demand; hiring and sourcing; on-boarding and integration; training and development; objective-setting and performance management; and compensation and rewards. What are we looking for? Work with the QA Lead to confirm that the appropriate style guide and client standards have been established for the client project(s). Learn the client's standards. Identify, track, and report on the quality status of client deliverables. Review project deliverables to ensure:oInstructional quality meets the defined objectives and product specifications, if applicable;oThey are free of spelling/grammatical/punctuation errors;oConciseness;oReduced repetition of information, unless specifically required by design, if applicable;oCompliance with agreed style guide and client standards (including tone/voice);oConsistency (formatting, use of terms, and so on), if applicable. Track and communicate errors in the defined categories for each deliverable. Provide feedback to the stakeholders. Work with the QA Lead in addressing barriers to quality development and coaching team members to address these gaps and improve quality. Provide reporting documents to the QA Lead as needed. Maintain a log of projects to ensure proper time tracking. A minimum of three years' experience in copy editing, proofreading, or reviewing instructional material, preferably in the digital medium. Proven knowledge of English grammar and different English dialects. Excellent command over written and verbal English, strong communication skills. Keen attention to detail. Familiarity with style guides such as the Chicago Manual of Style or in-house style guides. Proven expertise in using MS Office, mainly Word, PowerPoint, and Excel. Ability to work with stringent timelines; flexibility and agility to adjust to changing schedules. Ability to work with a range of subjects and client requirements. Ability to work independently with minimal direction. Roles and Responsibilities: In this role you are required to do analysis and solving of moderately complex problems May create new solutions, leveraging and, where needed, adapting existing methods and procedures The person would require understanding of the strategic direction set by senior management as it relates to team goals Primary upward interaction is with direct supervisor May interact with peers and/or management levels at a client and/or within Accenture Guidance would be provided when determining methods and procedures on new assignments Decisions made by you will often impact the team in which they reside Individual would manage small teams and/or work efforts (if in an individual contributor role) at a client or within Accenture Please note that this role may require you to work in rotational shifts Qualifications Any Graduation

We are seeking a highly motivated and detail-oriented Quality Assurance Engineer specializing in Process Control to join our team at DMW Universal Industries . The successful candidate will be responsible for ensuring the quality and consistency of our aluminium casting processes through effective process monitoring, control, and improvement. This role requires a strong understanding of aluminium casting principles, quality management systems, and statistical process control techniques Role & responsibilities Process Monitoring and Control: Develop, implement, and maintain process control plans for all stages of the aluminium casting process, including melting, pouring, solidification, and heat treatment. Monitor critical process parameters (e.g., temperature, pressure, flow rate, alloy composition) using appropriate measurement tools and techniques. Analyze process data to identify deviations from established specifications and implement corrective and preventive actions. Maintain accurate and up-to-date process control records Quality Management System (QMS): Ensure compliance with relevant quality standards (e.g., ISO 9001, AS9100) and customer requirements. Participate in internal and external audits. Develop and maintain quality documentation, including work instructions, procedures, and control plans. Assist in the development and implementation of QMS improvements Statistical Process Control (SPC): Apply SPC techniques to monitor and analyze process variability. Develop and interpret control charts (e.g., X-bar, R, p, c). Conduct capability studies to assess process performance. Use statistical analysis to identify root causes of process deviations Material Testing and Analysis: Oversee material testing, including chemical analysis, mechanical testing (e.g., tensile strength, hardness), and non-destructive testing (NDT). Analyze test results and provide recommendations for process adjustments. Maintain records of material test results Problem Solving and Continuous Improvement: Investigate quality issues and implement effective root cause analysis. Develop and implement corrective and preventive actions (CAPA). Participate in continuous improvement initiatives (e.g., Kaizen, Six Sigma). Work with production to reduce scrap and improve first pass yield Collaboration and Communication: Collaborate with production, engineering, and other departments to ensure quality objectives are met. Communicate quality-related information effectively to all stakeholders. Provide training and support to production personnel on quality procedures and process control techniques Preferred candidate profile Bachelor's degree in Metallurgical Engineering, Materials Science, Mechanical Engineering, or a related field Proven experience in quality assurance and process control in an aluminium casting foundry or similar manufacturing environment Strong understanding of aluminium casting processes and metallurgy Proficiency in using SPC tools and techniques Knowledge of quality management systems (ISO 9001, IATF). Experience with material testing and analysis Excellent problem-solving and analytical skills Strong communication and interpersonal skills Ability to work independently and as part of a team Experience with NDT methods Preferred Skills: Experience with lean manufacturing principles Benefits: Competitive salary and benefits package Opportunities for professional development and growth A dynamic and challenging work environment

Role & responsibilities:- Developing and implementing strategies to achieve business goals and objectives. Overseeing the company's day-to-day operations, including managing budgets, resources, and employees. Monitoring market and industry trends to determine business opportunities and challenges. Develop and maintain relationships with customers, vendors, and partners. Ensuring business compliance with relevant laws and regulations. Analysing data and performance metrics to make informed decisions.

Responsibilities: Quality Management System (QMS) Documentation Vendor Management Shade Card Management Regulatory Affairs Documentation Document Control & Compliance

Preparation of various procedure including Quality manual, QMS procedure, Work instruction, Testing procedure, NDE procedure as per customer specification & codes & standard.Inspection, Expediting, Verification & Certification of various Materials Required Candidate profile Diploma / BTech Mechanical with 20-25 yrs of exp. Age Minimum 50 yrs. Exp from Valve industry or any technical manufacturing industry.

QMS Consultant & Veeva Vault Project Support Analyst Role Overview We are seeking a professional with expertise in Quality Management Systems (QMS) and Veeva Vault to support the implementation, migration, and optimization of quality management processes. This role will focus on document and data migration, regulatory compliance, system integration, and ongoing support for Veeva Vault applications. The candidate will work from 5:30 PM IST 2:30 AM IST to align with the US time zone . Key Responsibilities Quality Management & Compliance Provide subject matter expertise on Vault R&D migration and quality management . Ensure quality standards, GxP compliance, and regulatory requirements (e.g., ISO 9001) are met. Conduct risk assessments to identify compliance gaps and inefficiencies. Define document classification and approval workflows aligned with industry best practices. Develop, implement, and maintain standard operating procedures (SOPs) and workflows for quality management. Manage change control processes , ensuring minimal disruption to quality standards. Implement post-migration quality checks to ensure document integrity. Provide ongoing monitoring and support for quality management tools and systems integrated with Veeva Vault. Track quality metrics, risks, and issues in compliance reports. Veeva Vault Implementation & Support Assist in migrating data and documents into Veeva Vault , ensuring accuracy and compliance. Collaborate with cross-functional teams to gather requirements and align migration activities with project goals. Provide technical expertise on Veeva Vault functionalities, workflows, integrations, and best practices . Conduct data quality checks post-migration to validate completeness and integrity. Troubleshoot technical issues and provide system support. Optimize automation, reporting, and regulatory compliance tracking within Veeva Vault. Communicate with both technical and non-technical teams to bridge business needs with system specifications. Identify, assess, and escalate potential risks related to migration and system integration. Training & Stakeholder Engagement Develop and update training documents and job aids for new Veeva Vault practices. Work alongside the Training & Procedures Team to provide comprehensive end-user training. Conduct product demonstrations and stakeholder engagement sessions to ensure seamless adoption. Gather and address stakeholder feedback to improve system functionalities and compliance adherence. Required Skills & Experience Technical & Functional Expertise 3+ years of experience in Veeva Suite, Veeva Vault, and Quality Management Systems (QMS) . Prior experience with Veeva migration support, data/document migration, and metadata mapping . Experience working with Veeva Vault Quality Suite , including workflows, document types, reports, dashboards, and notifications. Strong understanding of GxP, ISO 9001, and software validation regulations . Hands-on experience in testing, script execution, and system troubleshooting . Experience in configuring and resolving issues in multiple Veeva Vaults . Soft Skills & Qualifications Veeva Admin Certification is required . Bachelors degree in life sciences, computer science, or a related field . Strong analytical, problem-solving, and attention to detail skills. Excellent communication and interpersonal skills to work collaboratively across teams. Ability to influence stakeholders and manage change control processes effectively. Highly organized and detail-oriented with strong documentation skills. This role is ideal for candidates who can blend technical expertise with quality management practices while ensuring seamless regulatory compliance, data integrity, and system optimization within Veeva Vault.

SUMMARY Associate - Procurement (Purchase) Ahmedabad, INDIA Position Code: 1214AA About the Role: We are looking for an Associate - Procurement (Purchase), who thrives in a high performance and fast paced technical environment. As an Associate within the Procurement (Purchase) team, you will be responsible for independently performing most function tasks, ensuring that our customer receives a great product. What you'll deliver: Work to team plan & deliver your tasks on-time & within budget Evaluate your work progress to the plan and make required course corrections Compliance to company code of conduct in all purchase & store activities and immediately report non-compliance Support Purchase and store processes for consumable, capital goods and services Support "Request for Quotation" "Request for Proposal" documentation Support supplier selection, competitive bidding & offer evaluation process Support supply continuity risk mitigation framework Support goods receipt, store and inventory management framework Support Supplier compliance with statutory and customer requirements Optimise inventory and spend with demand forecast Support, Purchase orders, purchase agreements and rate contracts frameworks Work with Supply Chain and Finance function to fulfil organisation needs and swift payments Swiftly resolve non-conformance to minimise impact on project objectives Deliver your work 'right first time' & 'on time in full' Understand project goals and objectives and complete your task within budget Follow processes, standard operating procedure (SOP) and apply best practices in your work Follow function's performance and improvement processes in your work Apply lean & 5S visual work environment principles in your work Align your work to meet your KPIs to achieve your growth goals Evaluate your KPI trend and implement required course corrections Utilise learning material & proactively participate in discussion forums Make your learning program to enhance your skills & knowledge & competency Make & implement your performance & economic growth plan What you'll need: Passion for our Vision: Transform Manufacturing 2+ years of total working experience in related domain In-depth domain knowledge & competency gained at an education institution or self-learnt Proficient Knowledge & Competency of purchase & store organisation with P&L responsibilities Proficient Knowledge & Competency of purchase terms and conditions, bidding process & contracts Good analytical and negotiation skills in order to get the best price and value products and services Proficient Understanding & Competency of application taxes, customs duty & statutory compliances Development Knowledge & Competency of high verity low volume store & inventory management Proficient understanding & competency of quality management systems and ISO9001/AS9100 standards Proficient understanding & competency of lean & six sigma principles Proficiency in engineering fundamentals and emerging technologies Proficient ability to identify risks, manage them and implement mitigating actions Flexibility to go beyond normal work hours in time of need and support other functions Must have: Attitude to positively work with cross functional teams Respectful behaviour and willingness to adapt company code of conduct Attitude to learn, do your best work and grow Initiative and courage to explore new ideas and learn from the mistakes Perfectionist approach and meticulous to the finest detail in everything that you do Clear and concise written & verbal English language communication as well as presentation skills Prompt and on-time communication of operational matters Proficiency in Excel, Outlook, PowerPoint, Teams and other MS Office software Readiness work in different shifts to support customers in different time zone Nice to have: Experience in Engineering Purchase and Supply chain Experience of working with leading ERP software like - Epicor / SAP / NetSuite Great sense of humour

Purpose of the role: This position will form an integral part in achieving all quality objectives by developing & implementing the current Quality procedures and systems in line with global regulatory expectations and industry practices. Need to work closely with all CFT team in a collaborative manner to build a Quality system. Primary Responsibility: 1. Lead all personnel and processes involved in Inspection and Packaging operations occurring on all shifts. 2. Maintain knowledge of state-of-the-art Biopharmaceutical industry standards and guidelines for inspection and packaging concepts, practices, and processes. 3. Responsible for DP facility packing activities (operation and cleaning of Visual inspection board, Plunger rod insertion & Labelling machine, Cartridge Labelling machine, Blister packing machine, Automatic Cartoning Machine, Pen Assembling and labelling machine, Cold room) related to drug product. 4. Assist the installation and commissioning activities like FAT, SAT etc. of the packing lines for Vials, PFS and Cartridge facility packing. 5. Preparation and review of the URS, QRM, IQ, OQ and PQ protocols for Plunger rod insertion & Labelling machine, Cartridge Labelling machine, Blister packing machine, Automatic Cartoning Machine, weighing balances, Pen Assembling and labelling machine, Serialization etc. 6. Ensure QMS compliance in qualification, visual inspection and packing related activities. 7. Assist the validations of equipment and the process. 8. Identify and implement the visual inspection and packing procedures with compliance to current GMP requirements. 9. Implementation of Track & Trace system for the packaging. 10.Performing the FAT & SAT of packing line equipment at vendor sites or at our facility. 11. Performing/executing the IQ, OQ and PQ related to packaging lines. 12. Performing the visual inspection activities. 13. Assisting the validation activities of other equipment like cold room, pass-box and area. 14. Prepare & review of all SOP`s/protocols related to visual inspection/packing area procedures/equipment and drug product facility. 15. Identify and implement the manufacture procedures with compliance to current GMP requirements. 16. Timely initiation, investigation, impact assessment of QMS elements.

Dear Candidate, Greetings from Grupo Antolin India Pvt. Ltd. We are one of the largest players in the car interiors market internationally and number 1 worldwide supplier of headliner substrates. We offer products with high added value to outfit automobile interiors: Overhead Systems, Doors, Cockpits, Lighting, Electronic Systems & Integrated Products. We dominate the complete component cycle from component conception and design, through development and validation to parts industrialization and sequenced delivery. We have Multiple openings with us in " Quality Department" for our plant in CHAKAN PUNE. Manufacturing Quality Engineers - 1.Manufacturing Quality . 2.Customer Complaint & 8D report SCAP 3.Customer claims management. 4.Countermeasure Report. 5.Product & Process Changes. 6.PPAP, PFMEA & SPC. 7.Shift start Q-validation. 8.Production self-control, support and verification. 9.Flash & Product audits. 10.Internal rejection management. 11.5S audits shop floor. QMS Engineers (Preferably Females) - Knowledge of QMS. Knowledge of Process, Product, flash & IATF certification & their documentation. Customer Audit interface. Plant Internal audits plan & adherence. Monitor the effectiveness of the QMS and continuously improve. CSR Requirements evaluation and Update Lab Quality Engineers (Preferably Females) - 1.QA lab yearly validation and testing trials as per the Control plan management according to control plan. 2.Initial sample Approval and Part Inspection for new launches and running changes Parts. 3.Hands on experience of conducting the test and making the test reports and lit bit understanding of NABL Lab activities. Qualifications - Bachelors in Mechanical Engineering. Minimum of 4 to 9 years of experience in Quality function from automobile industry. What can we offer you: You will be part of a highly engaged multinational with international career opportunities. We offer you a learning journey adapted to your professional experience. You will work on international projects for world- renowned companies in Automotive sector. You can find an open Environment to learn new technologies. We can offer you a competitive salary & benefits. If you are interested for the said position, kindly revert back with your updated profile on below email Id - Megha.Aglawe@antolin.com.

Purpose of the role: Responsible for stability Management Primary Responsibility: Strategic: 1. Ensure 100% compliance to usage of Quality systems. Operational: 1. Adherence of cGMP (Current Good Manufacturing Practice) and cGLP (Current Good Laboratory Practice). 2. To have control and ensure the Stability team management. 3. To ensure the stability samples are analyzed and released as per schedule. 4. To ensure none of the stability samples are being crossed the window period. 5. Review of Stability samples in quality control department. 6. Instrument/Equipment qualification Review in Quality control. 7. Preparation and maintenance of quality records and study protocols. 8. Preparation of quality system related, Instrument operation related SOPs, Specification, STPs, URS etc. 9. Coordinate with cross functional teams such as Production, QA, Warehouse, SCM etc. 10. Review of method transfer and method validation in quality control. 11. Handling of QMS elements related to quality control. 12. Maintenance and calibration of instruments in Quality control. 13. Quality Interface in audits (both internal and external) and ensure appropriate QMS document identified in a timely manner and closed out. 14. Analysis of vendor samples and reporting. 15. Follow approved STPs, SOPs, and Specifications 16. To ensure readiness for Customer and regulatory audits. 17. Providing the support to meet the management objectives of product deliveries on time in line with Quality Management system. 18. Support quality related activities in other sites of Stelis (as required)

Handle Delivery Units / Horizontals / Accounts independently Carry out projects process audits to verify the compliances of projects. To interact with customers during client audits/evaluations. To participate in external audits and assist auditors from certifying bodies. Training project teams on QMS/Standards, Procedures, Guidelines and use of templates. Triggering process improvements & continuous improvements. Participation in process definition activities Process and Product Metrics collection, analysis and reporting Skill Required Good understanding of Quality Management system Excellent Team Management and Interaction with Senior Management Knowledge on ISO 9001, CMMI Good communications skills Presentation Skills to customers and auditors

Oversees a facility's QA/QC: Strategies Objectives Operational status to ensure high-quality processes and products Reviewing policies and procedures Ensuring compliance with regulatory standards

CSV Overall, 10 + Yrs. of experience in SAP CSV Validation Services. Developing validation strategies and plans for SAP implementations, upgrades, and modifications to ensure compliance with regulatory requirements. Conducting System GMP impact assessment, GAMP category assessment, ERES applicability assessment, Requirement/ Functional risk assessment after establishing communication with relevant stakeholders. Conducting change assessments and impact analyses to identify mandatory validation deliverables. Collaborating with cross functional teams, including IT, Business Process, CSV and Quality Assurance to ensure alignment on validation deliverables. Creation, execution, documentation, and review of validation plan, including FDS, BDS, TDS, test plan/ scripts, IQ/OQ/PQ Protocols, Traceability Matrix, validation reports and Release notification (Go Live). Support in defect management/ discrepancy investigation if any as part of the validation deliverables. Providing guidance and support to project teams on validation best practices and compliance requirements. Submit the complete Change/Incident/Project documentation with evidences for review and approvals by the business/quality teams. Upon acquiring all approvals, shall communicate to the development/transport/Basis teams to deploy the change/incident/project in Production environment. Ensure the change/incident/project in Production environment is deployed without any deviations. Participating in validation related meetings, training sessions. Participate in Governance reviews, status reporting and handling of escalations Keeping abreast of industry trends, regulatory changes, and best practices related to CSV in SAP. Contributing to the continuous improvement of validation processes and procedures within the organization. Support during Client Visit and Regulatory inspections.

Roles and Responsibilities: Lead and manage a quality team, ensuring high performance and engagement. Demonstrate strong skills in assessment, problem-solving, and policy administration/interpretation. Exhibit flexibility to quickly shift priorities, multitask, and manage simultaneous requirements in a fast-paced environment, ensuring all tasks are completed effectively. Maintain a process-oriented approach with strong organizational and prioritization skills. Interact with clients to understand key business priorities and identify opportunities for improvement. Collaborate with the broader Six Sigma community to tackle business challenges. Provide innovative leadership to drive quality performance across the organization. Direct the identification of gaps and implement improvements in various processes. Ensure the application of problem-solving techniques and root cause analysis where necessary. Deploy frameworks to enhance process performance on the shop floor. Work independently with minimal supervision, taking initiative and following up on assigned projects while fostering good partnership skills. Build strong relationships and effectively collaborate with individuals at all levels of the organization. Exhibit excellent communication, facilitation, and interpersonal skills. Proficient in Microsoft Office Suite, including Windows, Word, Excel, PowerPoint, and Visio. Manage day-to-day employee-related issues, providing appropriate resolutions. Coach, mentor, and motivate team members, fostering excellent employee engagement. Meet and exceed all expectations of the organization s Quality Management System (QMS). Process Specific Skills: Preferably knowledge of US Healthcare domain being aligned to Medical Billing & RCM (end to end). Lean Six Sigma GB Training / Certification from reputed organization / institute preferable Strong awareness and expertise in Quality Management Systems (QMS). Knowledgeable in quality tools and concepts. Excellent people management skills. Strong communication and presentation abilities.

As a Senior Engineer in the Coating department, you will be responsible for overseeing all aspects of quality control in the coating process. This includes ensuring that all products meet the required quality standards and specifications. You will be responsible for implementing and maintaining quality management systems and product certification processes. You will also be responsible for conducting various types of testing, including destructive and non-destructive testing, to ensure product quality. Oversee and manage the coating process to ensure quality and consistency. Implement and maintain Quality Management Systems and Product Certification processes. Utilize metrology tools and techniques to measure and analyze coating quality. Conduct both destructive and non-destructive testing to assess the quality of coatings. Carry out regular inspections and audits to ensure adherence to quality standards. Apply Total Quality Management (TQM) principles and practices to improve processes and increase efficiency. Stay updated with the latest API and ISO standards for pipe manufacturing and ensure their implementation. Lead with vision and customer focus, ensuring that all actions taken align with the company's goals and customer expectations. Manage resources effectively and encourage interdependencies within the team to ensure smooth operations. Maintain a strong focus on Quality Health Safety & Environment Orientation. Show commitment to the organization's objectives and values. Solve problems effectively and efficiently, using strong analytical thinking and process orientation skills. Act as a functional expert in Operation and QA/QC for the Pipe Industry, providing guidance and support to other team members. Demonstrate a global mindset, business & commercial acumen, people excellence, and entrepreneurship in all tasks and responsibilities. This role requires a dynamic individual who can balance technical expertise with strong interpersonal skills to ensure the highest quality of our products and the satisfaction of our customers.

Role & responsibilities Internal Business Process- To establish systems and procedures to ensure that the process, product and service quality leads to the satisfaction of the customer. To ensure towards making the department a system driven. To ensure availability of various materials in time to meet OTIF. To ensure that required resources in the department. Promote innovation and changes in dept. to improve business performance. Customer Satisfaction- Ensure Reduction in customer complaints Ensure OTIF Ensure fulfill the all customers requirements/query/documents Ensure customer satisfaction during plant visit/audit People Development- Ensure Training need identification (TNI) and provide training accordingly. Safety Compliance- Ensuring Zero Incidents and Lost Time Injury. Compliance to Job Safety Plan & SOPs. Ensuring Compliance to SOP by conducting Safety Observation Visits. Ensure Contractor Site Safety Audits. Ensure proper working conditions for safe working of own and contractor Preferred candidate profile Perks and benefits

Job Description Summary Develop and maintain systems, rules, and processes to ensure fulfillment of internal and external requirements. Ensures that projects and products are capable and will meet specified standards (Preventive). Has knowledge of best practices and how own area integrates with others; is aware of the competition and the factors that differentiate them in the market Job Description Roles and Responsibilities GEHC ONLY Creates a Quality culture by driving compliance activities around a specific product, site or region. This includes being responsible for the total quality management system for the business and driving Quality metrics. Ensures quality and regulatory compliance while driving process effectiveness and efficiency. Represents GE Healthcare to external agencies and champions the evolution of the quality culture which includes executing and driving quality objectives, metrics, reporting and operating mechanisms. Utilizes in-depth knowledge of a discipline and analytical thinking to execute policy/strategy. Basic knowledge of related job disciplines. Acts as a resource for colleagues with less experience. May lead small projects with low risks and resource requirements. Explains information; developing skills to bring team members to consensus around topics within field. Conveys performance expectations and may handle sensitive issues. Jobs at this level function with some autonomy but are subject to functional practices and precedents or are covered by well-defined policies or review of end results. The job allows modification of procedures and practices covering work as long as the end results meet standards of acceptability (quality, volume, timeliness etc.). Uses some judgment and has the ability to propose different solutions outside of set parameters to address more complicated, day-to-day problems. Has ability to prioritize information for data analysis. Uses technical experience and analytical thinking. Uses multiple internal and limited external sources outside of own team to arrive at decisions. Required Qualifications This role requires advanced experience in the Quality Healthcare Quality. Knowledge level is comparable to a Bachelors degree from an accredited university or college with minimum of 8 years of experience in healthcare domain. Desired Characteristics Advance knowledge on ISO 13485 and Medical device regulations and standards for MDSAP countries for eg. FDA 21 CFR, EU MDR. Inclusion and Diversity GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you d expect from an organization with global strength and scale, and you ll be surrounded by career opportunities in a culture that fosters care, collaboration and support . Additional Information Relocation Assistance Provided: Yes

Job Description Summary Develop and maintain systems, rules, and processes to ensure fulfillment of internal and external requirements. Ensures that projects and products are capable and will meet specified standards (Preventive). In-depth understanding of key business drivers; uses this understanding to accomplish own work. In-depth understanding of how work of own team integrates with other teams and contributes to the area. Job Description Roles and Responsibilities Creates a Quality culture by driving compliance activities around Digital/Software products that may nor may not be for medical applications, and for certain sites or regions. This includes being responsible for the total quality management system for the business and driving Quality metrics. Ensures quality and regulatory compliance while driving process effectiveness and efficiency. Represents GE Healthcare to external agencies and champions the evolution of the quality culture which includes executing and driving quality objectives, metrics, reporting and operating mechanisms. Developing in-depth knowledge of a discipline. Uses prior experience and acquired expertise to execute functional policy/strategy. This is an individual contributor, with proven interpersonal skills. Communication with direct colleagues and the business about design and coordination services rendered. Provides informal guidance to new team members. Explains complex information to others in straightforward situations. Impacts projects, processes and procedures in own field. The role operates with some autonomy, but is focused on execution of activities/provision of advice within an enabling discipline covered by standard functional practices and procedures. Activities require professional judgment, but may require more senior levels of guidance. Utilizes technical expertise and judgement to solve problems. Leverages technical skills and analytic thinking required to solve problems. May use multiple internal sources outside of own team to arrive at decisions. Required Qualifications This role requires advanced experience in the Quality Healthcare Quality. Knowledge level is comparable to a Bachelors degree from an accredited university or college ( or a high school diploma with relevant experience). Experience with driving quality assurance and compliance for Digital/Software products. Experience key QMS elements- including but not limited to CAPA, Risk Management and Design Controls. Desired Characteristics Experience in AI/ML/Data Science. Experience in Cybersecurity and Privacy Additional Information Relocation Assistance Provided: No

Designation: Associate Manager QA Job Location : Mangalore Department: MSEZ- Quality Assurance About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve RD productivity, speed up time to market and lower the cost of innovation. Job Purpose: Associate Manager - Quality Assurance to manage QMS activities Educational Qualification: M.Sc. (Chemistry), B Pharma/M Pharma or any other equivalent university degree. Experience: 8 to 12 Years Technical Skill: Participation in regulatory inspections and audits and managing responses and corrective actions. Ensuring compliance with data integrity policy and identifying the cause of non-compliance. Responsible for all engineering quality assurance activities and not limited to: Review and approval of Calibration / PM planners and schedule/ Engineering and Maintenance documents/ SOPs of Engineering and Maintenance. Review and approval of Information Technology related documents Handling of LMS Training Activities. Compilation and Preparation of Quarterly QMS trends Preliminary review of Quality notifications (such as Change control, Deviation, CAPA, Customer complaints, OOS, OOT) for its completeness and correctness. Preparation and review of Quality Agreement. Client communication. Vendor Qualification. Preparation and/or review and/or approval of Standard Operating procedures and ensuring the adherence to the guiding SOP. Review and approve of equipment qualification and engineering related validation documents for its adequacy and accuracy. Reviewing the risk assessments for its adequacy and accuracy. Familiar with Trackwise, EDMS, SAP and LMS applications. Key Responsibilities: Establishing and maintaining a robust QMS in accordance with regulatory requirements (e.g., ICH, FDA, EMA). Management of Site QMS and trending. Management of document archival. Site Training coordinator. Technical/functional Skills: Good communication skills and experience in API industry. Behavioural Skills: Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team. Good speaking-listening-writing skills, attention to details, proactive self-starter. Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Should be able to work in team and flexible for working in shifts. Should be a focused employee. Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Identification ofTraining needs, Content Development, and expertise in delivery & Implementation. Assess trainingneeds through surveys, interviews with employees, or consultations withmanagers or instructors. Train and evaluateHO, Regional and ground/on-field resources; primary focus will be on"on-field" resources. Measuring trainingeffectiveness Requirements 5 years in Trainingdepartment preferably from Aviation or Retail Industry, Expertise in soft skills, communication, ability for specific detailing andteam building Should be able tospeak at least 2-3 regional languages viz Bengali/Assamese/Oriya etc. Should be open totravel across the East region of India Experience inTraining Blue Collar workers would be an added advantage, Candidates with Sports/events background will be considered. Minimum graduatewith training certifications from reputed institutes Candidates havingmilitary family background would be preferred. Candidateshaving QMS certification would be preferred.